drugset / Trial / NCT01983124

Vemurafenib + Fotemustine to Treat Advanced Melanoma Patients With V600BRAF Mutation Recurred While on Vemurafenib

NCT01983124

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the activity of Vemurafenib in combination with Fotemustine in Patients with unresectable Stage IV melanoma harboring V600 BRAF mutation who recurred while in treatment with Vemurafenib. In addition the feasibility and safety profile of prolonging treatment of this drugs combination will be assessed.

Timeline

Start
2013-02
Primary completion
2014-04
Completion
2015-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Vemurafenib Small molecule 480 mg Oral
Subject Vemurafenib Small molecule 720 mg Oral
Subject Vemurafenib Small molecule 960 mg Oral
Subject fotemustine Small molecule 100 mg/m2 Intravenous

Indications